Clinical trial · Expanded Access
Yttrium Y 90 Radiolabeled Glass Beads in Treating Patients With Liver Cancer That Cannot Be Removed by Surgery
A Treatment of Unresectable Hepatocellular Carcinoma With TheraSphere (Yttrium-90 Glass Microspheres): A HDE Treatment Use Protocol
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Internal radiation therapy uses radioactive material placed directly into or near a tumor to kill tumor cells. Using radiolabeled glass beads to kill tumor cells may be effective treatment for liver cancer that cannot be removed by surgery. PURPOSE: To provide expanded access and study the side effects of yttrium Y 90 glass microspheres in treating patients with liver cancer that cannot be removed by surgery.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Liver Cancer | Malignant Liver Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| brachytherapy | Radiation | — | UNRESOLVED |
| yttrium Y 90 glass microspheres | Radiation | — | UNRESOLVED |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Confirmed diagnosis of hepatocellular carcinoma * Surgical evaluation by a member of the Liver Tumor Program must conclude the patient is not a candidate for resection or ablation * Eastern Cooperative Oncology Group (ECOG) Performance Status Score 0-2 * Able to comprehend and provide written informed consent in accordance with institutional and federal guidelines Exclusion Criteria: * Absolute granulocyte count =\<1,500/ul * Platelet count =\<75,000/ul * Serum creatinine \>= 2.0 mg/dl * Serum bilirubin * \>= 2.0 mg/dl for bilateral treatment or lobar treatment * \>= 3.0 mg/dl for single lesion which could be treated by segmental fusion * History of severe allergy or intolerance to any contrast media, narcotics, sedatives, or atropine * Bleeding, diathesis not correctable by usual forms of therapy * Severe peripheral vascular disease that would preclude catheterization * Portal hypertension with portal venous shunt away from the liver * Evidence of potential delivery greater than 16.5 mCi (30 Gy absorbed dose) of radiation to the lungs on either: 1. first TheraSphere administration; or 2. cumulative delivery of radiation to the lungs \> 30 Gy over multiple treatments * Evidence of any detectable Tc-99m MMA flow to the stomach or duodenum, after application of established angiographic techniques to stop such flow * Significant extrahepatic disease representing an imminent life-threatening outcome * Severe liver dysfunction (Childs' Classification C) or pulmonary insufficiency (requiring continuous oxygen therapy) * Active uncontrolled infection * Significant underlying medical or psychiatric illness * Pregnant women may not participate * Children may not participate
References
Publications (0)
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